Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 7:34782027 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 20 HGVS names - click the plus to show

7:g.34782027C>T
ENST00000381544.2:c.280+57731C>T
ENST00000436945.3:n.268-13599G>A
ENST00000535640.1:n.165-13599G>A
ENST00000381539.3:c.281-36047C>T
ENST00000442669.2:n.274-13599G>A
ENST00000381553.3:c.281-36047C>T
ENST00000360581.1:c.281-36047C>T
ENST00000358772.4:n.200-13599G>A
ENST00000419766.1:n.81-13599G>A
ENST00000359791.1:c.281-36047C>T
ENST00000544556.1:n.200-13599G>A
ENST00000537560.1:n.200-13599G>A
ENST00000531252.1:c.281-36080C>T
ENST00000431669.1:n.165-13599G>A
ENST00000381542.1:c.280+57731C>T
ENST00000396095.2:c.281-36047C>T
ENST00000428922.1:n.81-13599G>A
ENST00000439852.1:n.200-13599G>A
ENST00000539747.1:n.85-13599G>A

Variation displays